5.01.d
Disorders of niacin and NAD metabolism
- Nicotinamide mononucleotide adenylyl transferase 1 deficiency (Leber congenital amaurosis 9)
- NAD synthetase 1 deficiency (Vertebral, cardiac, renal, and limb defects syndrome type 3)
- Mitochondrial NAD kinase 2 deficiency (2,4-dienoyl-CoA reductase deficiency with hyperlysinemia)
- NAD(P)HX dehydratase deficiency (CARKD deficiency)
- NAD(P)HX epimerase deficiency (Apolipoprotein A-I binding protein deficiency)
- Nicotinamide nucleotide transhydrogenase deficiency (Glucocorticoid deficiency type 4)
Subnetworks
NOMS
Disorders of neuromodulators and other small molecules
